8.55060

Rink Acid resin (100-200 mesh)

Novabiochem®

Manufacturer: Sigma Aldrich

Synonym(S): 4-(2′,4′-Dimethoxyphenyl-hydroxymethyl)-phenoxy resin

Select a Size

Pack Size SKU Availability Price
1 G 8.55060-1-G In Stock ₹ 3,910.47
5 G 8.55060-5-G In Stock ₹ 16,550.00

8.55060 - 1 G

₹ 3,910.47

In Stock

Quantity

1

Base Price: ₹ 3,910.47

GST (18%): ₹ 703.885

Total Price: ₹ 4,614.355

Quality Level

200

product line

Novabiochem®

form

beads

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

manufacturer/tradename

Novabiochem®

application(s)

peptide synthesis

functional group

alcohol

storage temp.

2-30°C

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Description

  • General description: Rink acid resin is a super acid-labile support for the solid phase immobilization of carboxylic acids [1] by Fmoc SPPS. Cleavage can be effected with as little as 10% AcOH in DCM, providing highly acid-sensitive products in high yields and purities. However, care must be taken to prevent product loss during synthetic manipulations [2], owing to the extreme acid sensitivity of this support. Treatment with HCl in THF [3] or Ph2PCl2 [4] has been shown to efficiently convert this resin to the corresponding benzhydryl chloride, to which can be coupled a wide range of functional groups: hydroxylamines [3], alcohols, amines, acids and thiols [4]. Rink acid resin has also been converted to a trifluoroacetate with TFA and used in a similar manner to immobilize amines, thiols, alcohols, and phenols [5]. In a more detailed study, the same authors found 1 M trifluoroacetic anhydride in 2,6-lutidine to give superior results with less degradation of the linker [6, 7]. Rink resin trifluoroacetate has also been used to prepare purines [8, 9].Cleavage of amines and alcohols from this support has been carried out with either 5% TFA in DCM [4] or 20% TFA in DCM [5]; thiols were released with either 5% TFA in DCM [4] or 95% aq. TFA [5].Associated Protocols and Technical Articles Protocols for Loading of Peptide Synthesis Resins Literature references [1] H. Rink (1987) Tetrahedron Lett., 28, 3787. [2] H. U. Immer, et al. in ′Peptides, Chemistry, Structure &Biology, Proc. 11th American Peptide Symposium′, J. E. Rivier & G. R. Marshall (Eds), ESCOM, Leiden, 1990, pp. 1054. [3] S. L. Mellor & W. C. Chan (1997) J. Chem. Soc., Chem. Commun., 2005. [4] R. S. Garigipati (1997) Tetrahedron Lett., 38, 6807. [5] W.K.-D. Brill in ′First Conference on Synthetic Organic Chemistry′, www.mdpi.org/ecsoc, 1997. [6] W.K.-D. Brill (1998) Syn. Lett., 906. [7] R. A. Tommesi, et al. (1998) Tetrahedron Lett., 39, 5477. [8] W.K.-D. Brill (2001) Syn. Lett., 1097. [9] W.K.-D. Brill & C. Riva-Toniolo (2001) Tetrahedron Lett., 42, 65`5.
  • Linkage: Replaces: 01-64-0012
  • Analysis Note: Color (visual): white to yellow to beigeAppearance of substance (visual): beadsLoading (determined from the substition of the Fmoc-NH2 loaded resin): 0.35 - 0.80 mmol/gSwelling Volume (in DMF): lot specific resultThe polymer matrix is copoly (styrene - 1% DVB) 100 -200 mesh
  • Legal Information: Novabiochem is a registered trademark of Merck KGaA, Darmstadt, Germany

SAFETY INFORMATION

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Quality Level:
200

product line:
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form:
beads

reaction suitability:
reaction type: Fmoc solid-phase peptide synthesis

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Novabiochem®

application(s):
peptide synthesis

functional group:
alcohol

storage temp.:
2-30°C

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application(s):
peptide synthesis

functional group:
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storage temp.:
2-8°C

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200

product line:
NovaSyn® TGNovabiochem®

form:
beads

reaction suitability:
reaction type: Fmoc solid-phase peptide synthesis

manufacturer/tradename:
Novabiochem®

application(s):
peptide synthesis

functional group:
alcohol

storage temp.:
2-30°C

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Quality Level:
200

product line:
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form:
beads

reaction suitability:
reaction type: Boc solid-phase peptide synthesis

manufacturer/tradename:
Novabiochem®

application(s):
peptide synthesis

functional group:
alcohol

storage temp.:
2-30°C